A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17497937



Internal ID22555871
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:88071015..88086468hg38UCSC Ensembl
chr4:88992167..89007620hg19UCSC Ensembl
Cytoband4q22.1
Allele length
AssemblyAllele length
hg3815454
hg1915454
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5840428
Supporting Variants
Samples
Known GenesPKD2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17497937
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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